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Disease Ontology Browser
nuclear type mitochondrial complex I deficiency 16 (DOID:0112096)
Alliance: disease page
Synonyms: 'MC1DN16'
Alt IDs: OMIM:618238
Definition: A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in NDUFAF5 on chromosome 20p12.1.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
06/14/2022
MGI 6.19
The Jackson Laboratory